CTRI/2019/10/021495已完成未知
Clinical, Biochemical and Genetic profile of Patients with Congenital Adrenal Hyperplasia due to 11-βHydroxlase deficiency.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- A
- 入组人数
- 13
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Patients with Congenital adrenal hyperplasia due to 11-βhydroxylase deficiency.
排除标准
- •1)Patients with clinical characteristics of 11-β hydroxylase deficiency withoutconfirmed genetic diagnosis.
- •2)Inadequate Biochemical data.
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